Valsartan impurity E is a chemical compound used as a pharmaceutical reference standard for analytical testing. It is structurally related to the active pharmaceutical ingredient valsartan and is employed in quality control to ensure the purity and consistency of valsartan drug substances.
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
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CAS 137863-17-3
Valsartan benzyl ester
pharmaceutical intermediate
Valsartan
pharmaceutical raw material
D-valsartan
pharmaceutical raw material
Despentanoyl butanoyl valsartan
pharmaceutical raw material
N-(²H₉)Pentanoyl-N-{[2'-(2H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl}-L-valine
pharmaceutical raw material
Phenyl (3R,4R)-4-(3-isopropoxyphenyl)-3,4-dimethylpiperidine-1-carboxylate
pharmaceutical raw material
Octreotide Impurity 13
pharmaceutical raw material
Alogliptin Impurity 14
pharmaceutical raw material
methyl (2S)-3-methyl-2-[pentanoyl-[[4-[2-(2H-tetrazol-5-yl)phenyl]phenyl]methyl]amino]butanoate
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